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9342

CC(C)NCCS(=O)(=O)Cc1ccccc1.Cl
Reaction #4303
white crystalline solid
Выход 65.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Sc2ncccc2C1=O
Reaction #4908
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-thiazepin-5(4H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Sc2ncccc2C1=S
Reaction #4909
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-thiazepine-5(4H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC1CN(C)C(=O)c2cccnc2S1.Cl.Cl
Reaction #4930
2-[2-(Dimethylamino)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-thiazepin-5(4H)-one dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
SCCNCc1ccc(Cl)nc1
Reaction #50502
N-(2-chloro-5-pyridylmethyl)2-aminoethanethiol
Выход 82.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cn1nnnc1C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(N)[C@H]2SC1
Reaction #54321
benzhydryl 7-amino-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate hydrochloride
Выход 57.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=S)SC(C[N+](=O)[O-])c1ccc(Cl)cc1Cl
Reaction #54417
2,4-dichloro-α-(nitromethyl)-benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=S)SC(C[N+](=O)[O-])c1cc([N+](=O)[O-])ccc1Cl
Reaction #54422
2-chloro-5-nitro-α-(nitromethyl)benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=S)SC(C[N+](=O)[O-])c1ccccc1Cl
Reaction #54426
o-chloro-α-(nitromethyl)benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CSCCN1C(=O)Nc1ccc(Cl)cc1
Reaction #55284
3-carbethoxy-4-(4-chlorophenylaminocarbonyl)thiomorpholine
Выход 30.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(CCCC2SCC(=O)N2CCC2=CCCCC2)cc1Cl
Reaction #56491
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.O=[SH](=O)Nc1ccccc1
Reaction #69034
title compound
Выход 72.5%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)CCN1C(=O)c2ccccc2C1=O
Reaction #69035
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCS(=O)(=O)N1CCOCC1
Reaction #69036
2-(2-(morpholinosulfonyl)ethyl)isoindole-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.O=[SH](=O)Nc1ccc(I)cc1
Reaction #69037
2-phthalimidoethane N-(4-iodophenyl)sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.CN[SH](=O)=O
Reaction #69039
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.CN(C)[SH](=O)=O
Reaction #69040
2-phthalimidoethane N,N-dimethylsulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1csc(-c2ccccc2O)n1)NC1C(=O)N2C(C(=O)O)=C(Cl)CSC12
Reaction #81857
9b
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)Cn1nnnc1S
Reaction #173580
DOI: 10.1039/C8SC04228D
O=C1CSC(c2cccc(Cl)c2)c2cc(C(=O)c3ccc(Cl)cc3)ccc2N1
Reaction #174392
DOI: 10.1039/C8SC04228D
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